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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248354Generated: October 31, 2026

Iodine → α-3-Buten-1-yl-2,4-difluorobenzenemethanol

https://huagongshe.com/reaction/2248354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHomoallyl bromideHCID 21241—
Reactant2,4-DifluorobenzaldehydeHCID 73770—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Productα-3-Buten-1-yl-2,4-difluorobenzenemethanolHCID 14994860—

Reaction Steps

To a stirred suspension of magnesium turnings (16.9 gm) in dry diethyl ether (1.5L) was added (argon atmosphere) a crystal of iodine and 4-bromobutene (2 ml). Soon after the reaction was initiated the remaining 4-bromobutene (101 gm) in dry diethyl ether (500 mL) was added at such a rate to maintain gentle reflux. After complete addition, the mixture was heated to reflux for 1 hour. 2,4-Difluorobenzaldehyde (100 gm) in dry diethyl ether (400 mL) was then added dropwise with a gentle reflux. The mixture was now heated for 2 hours and allowed to cool to room temperature. The entire contents of the flask were poured on 6L ice-water containing 200 ml concentrated HCl. The organic phase was separated, washed with water, saturated NaHCO3, water and dried (Na2SO4). Removal of ether in vacuo provided crude 5-hydroxy-5-(2,4-difluorophenyl)pentene as an oil (136.5 gm) which was used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039676
Source datasetuspto-grants-1991_08
ORD IDord-d8008988cc3c4c2c959e4e070e990700
Source noteuspto-grants-1991_08